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Acapela Group Demo
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The User of this demo undertakes to use the demo in accordance with customs and standard practices. the User shall ensure that the demo will not be used to create prompts which are unlawful, harmful, threatening, abusive, harassing, tortuous, defamatory, vulgar, obscene, libellous, invasive of another's privacy, hateful, or racially, ethnically or otherwise objectionable.

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Speech impairment: Acapela Group introduces ‘my-own-voice’, a world premiere for voice replacement, in 10 languages.

Users about to lose the ability to speak with their own voice can now re-create it synthetically, enabling them to keep this essential part of their identity.
AcapelaGroup - MyOwnVoice

Acapela Group, speech expert and leading innovator in speech solutions, is launching a breakthrough service allowing users diagnosed with speech or language disorders (resulting from ALS or other conditions such as aphasia, dysarthria or apraxia) to capture the essence of their voice before losing it. This ground breaking invention will enable users to keep speaking with their own voice rather than having to use a standard anonymous synthetic voice. We simply call it ‘my-own-voice’.

 

‘Acapela Group is a bespoke player in speech solutions. For decades we have been creating well known synthetic voices used by visually impaired users. Accessibility issues are very important to Acapela and we work hard to make communication much easier for people with sight, speech and cognitive disabilities’ says Lars-Erik Larsson, CEO of Acapela Group. ‘For years we have been receiving requests from users or their relatives and until today the only answer we could give was ‘’we are working on it’’. We are very proud today to announce that we have created a service to meet this specific, crucial need. We know that once diagnosed the user doesn’t have much time to capture the essence of their voice before losing it. Our goal was to develop the most convenient service for them to use, while ensuring that all the sounds we need to create a synthetic version of their voice could be recorded. My-own-voice is a first step for us in the field of speech impairment. We look forward to developing further innovative solutions to help improve the lives of users,’ he adds.

The recording process

To allow individuals to capture their own voice, the first challenge for our R&D team was to create an entire, whole new process to enable recordings to be made by non-professional speakers, without any help from Acapela linguists, but with the support of the user’s speech therapist. Our expert knowledge had to be harnessed to an end user approach. It has worked out well. We have already run a couple of trials with users about to lose their voice. We have created the foundation for major progress for speech impaired people and we are working on improving methodology and tools to take this vital work forward.

Meet Eric and Garmt,

the pioneers of ‘my-own-voice’

Eric and Garmt have both been diagnosed with ALS. They have decided to create their own synthetic voice and have participated as pioneers on the first  ‘my-own-voice’ experiences.

Text-to-speech literally transforms any written input into an audio result. It means that ‘my-own-voice’, based on the recordings of a corpus of various texts, will be capable of speaking any text, as any synthetic voice can do.

 

Today, the my-own-voice website is ready to record, fully guiding the user and the speech therapist through the full process, based on everyday materials and adapted to those without any specific knowledge of speech technology. As proof of our commitment and strong belief in this project, my-own-voice will be free to create at an initial stage. A charge will be made only if the user is happy and comfortable with their synthetic voice and wants personal unlimited use (android or windows versions).
More information about my-own voice

 

Supporting ALS research

To reinforce our dedication to speech impaired users, Acapela Group is supporting Project MinE with a donation of 5% of the ‘my-own-voice’ revenues to help them reach their objective to map the full DNA profiles of 15,000 people with ALS, to perform comparative analyses on the resulting data, understand the genetic basis of ALS and better fight this neuromuscular disease.

 

More information

Project MinE

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